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Calreticulin expression and localization in relation to exchangeable Ca(2+) during pollen development in Petunia

BACKGROUND: Pollen development in the anther in angiosperms depends on complicated cellular interactions associated with the expression of gametophytic and sporophytic genes which control fundamental processes during microsporo/gametogenesis, such as exo/endocytosis, intracellular transport, cell si...

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Autores principales: Suwińska, Anna, Wasąg, Piotr, Bednarska-Kozakiewicz, Elżbieta, Lenartowska, Marta, Lenartowski, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742381/
https://www.ncbi.nlm.nih.gov/pubmed/34998378
http://dx.doi.org/10.1186/s12870-021-03409-4
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author Suwińska, Anna
Wasąg, Piotr
Bednarska-Kozakiewicz, Elżbieta
Lenartowska, Marta
Lenartowski, Robert
author_facet Suwińska, Anna
Wasąg, Piotr
Bednarska-Kozakiewicz, Elżbieta
Lenartowska, Marta
Lenartowski, Robert
author_sort Suwińska, Anna
collection PubMed
description BACKGROUND: Pollen development in the anther in angiosperms depends on complicated cellular interactions associated with the expression of gametophytic and sporophytic genes which control fundamental processes during microsporo/gametogenesis, such as exo/endocytosis, intracellular transport, cell signaling, chromatin remodeling, and cell division. Most if not all of these cellular processes depend of local concentration of calcium ions (Ca(2+)). Work from our laboratory and others provide evidence that calreticulin (CRT), a prominent Ca(2+)-binding/buffering protein in the endoplasmic reticulum (ER) of eukaryotic cells, may be involved in pollen formation and function. Here, we show for the first time the expression pattern of the PhCRT1 gene and CRT accumulation in relation to exchangeable Ca(2+) in Petunia hybrida developing anther, and discuss probable roles for this protein in the male gametophyte development. RESULTS: Using northern hybridization, western blot analysis, fluorescent in situ hybridization (FISH), immunocytochemistry, and potassium antimonate precipitation, we report that PhCRT1 is highly expressed in the anther and localization pattern of the CRT protein correlates with loosely bound (exchangeable) Ca(2+) during the successive stages of microsporo/gametogenesis. We confirmed a permanent presence of both CRT and exchangeable Ca(2+) in the germ line and tapetal cells, where these factors preferentially localized to the ER which is known to be the most effective intracellular Ca(2+) store in eukaryotic cells. In addition, our immunoblots revealed a gradual increase in CRT level from the microsporocyte stage through the meiosis and the highest CRT level at the microspore stage, when both microspores and tapetal cells show extremely high secretory activity correlated with the biogenesis of the sporoderm. CONCLUSION: Our present data provide support for a key role of CRT in developing anther of angiosperms – regulation of Ca(2+) homeostasis during pollen grains formation. This Ca(2+)-buffering chaperone seems to be essential for pollen development and maturation since a high rate of protein synthesis and protein folding within the ER as well as intracellular Ca(2+) homeostasis are strictly required during the multi-step process of pollen development. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-021-03409-4.
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spelling pubmed-87423812022-01-10 Calreticulin expression and localization in relation to exchangeable Ca(2+) during pollen development in Petunia Suwińska, Anna Wasąg, Piotr Bednarska-Kozakiewicz, Elżbieta Lenartowska, Marta Lenartowski, Robert BMC Plant Biol Research BACKGROUND: Pollen development in the anther in angiosperms depends on complicated cellular interactions associated with the expression of gametophytic and sporophytic genes which control fundamental processes during microsporo/gametogenesis, such as exo/endocytosis, intracellular transport, cell signaling, chromatin remodeling, and cell division. Most if not all of these cellular processes depend of local concentration of calcium ions (Ca(2+)). Work from our laboratory and others provide evidence that calreticulin (CRT), a prominent Ca(2+)-binding/buffering protein in the endoplasmic reticulum (ER) of eukaryotic cells, may be involved in pollen formation and function. Here, we show for the first time the expression pattern of the PhCRT1 gene and CRT accumulation in relation to exchangeable Ca(2+) in Petunia hybrida developing anther, and discuss probable roles for this protein in the male gametophyte development. RESULTS: Using northern hybridization, western blot analysis, fluorescent in situ hybridization (FISH), immunocytochemistry, and potassium antimonate precipitation, we report that PhCRT1 is highly expressed in the anther and localization pattern of the CRT protein correlates with loosely bound (exchangeable) Ca(2+) during the successive stages of microsporo/gametogenesis. We confirmed a permanent presence of both CRT and exchangeable Ca(2+) in the germ line and tapetal cells, where these factors preferentially localized to the ER which is known to be the most effective intracellular Ca(2+) store in eukaryotic cells. In addition, our immunoblots revealed a gradual increase in CRT level from the microsporocyte stage through the meiosis and the highest CRT level at the microspore stage, when both microspores and tapetal cells show extremely high secretory activity correlated with the biogenesis of the sporoderm. CONCLUSION: Our present data provide support for a key role of CRT in developing anther of angiosperms – regulation of Ca(2+) homeostasis during pollen grains formation. This Ca(2+)-buffering chaperone seems to be essential for pollen development and maturation since a high rate of protein synthesis and protein folding within the ER as well as intracellular Ca(2+) homeostasis are strictly required during the multi-step process of pollen development. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-021-03409-4. BioMed Central 2022-01-08 /pmc/articles/PMC8742381/ /pubmed/34998378 http://dx.doi.org/10.1186/s12870-021-03409-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Suwińska, Anna
Wasąg, Piotr
Bednarska-Kozakiewicz, Elżbieta
Lenartowska, Marta
Lenartowski, Robert
Calreticulin expression and localization in relation to exchangeable Ca(2+) during pollen development in Petunia
title Calreticulin expression and localization in relation to exchangeable Ca(2+) during pollen development in Petunia
title_full Calreticulin expression and localization in relation to exchangeable Ca(2+) during pollen development in Petunia
title_fullStr Calreticulin expression and localization in relation to exchangeable Ca(2+) during pollen development in Petunia
title_full_unstemmed Calreticulin expression and localization in relation to exchangeable Ca(2+) during pollen development in Petunia
title_short Calreticulin expression and localization in relation to exchangeable Ca(2+) during pollen development in Petunia
title_sort calreticulin expression and localization in relation to exchangeable ca(2+) during pollen development in petunia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742381/
https://www.ncbi.nlm.nih.gov/pubmed/34998378
http://dx.doi.org/10.1186/s12870-021-03409-4
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